- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT05407909
To Evaluate the Safety and Tolerability of SYHX2001 in Patients With Advanced or Metastatic Solid Tumors
8 augusti 2022 uppdaterad av: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
This is a Phase 1, open-label, multicenter, dose escalation and expansion study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of the experimental drug(SYHX2001) in previously treated patients with advanced or metastatic cancer.
Studieöversikt
Status
Rekrytering
Betingelser
Intervention / Behandling
Detaljerad beskrivning
This is a multicenter, open-label, dose-escalation, dose-expansion Phase 1 study of SYHX2001(name of the experimental drug) in patients with advanced or metastatic cancers who have exhausted standard treatment.
The study will consist of 2 parts, a dose escalation part and a cohort expansion part.
Once the recommended phase 2 dose (RP2D) has been determined in the dose escalation part, a cohort expansion part involving up to three separate cohorts will be conducted.
For patients, the study will include a screening phase, a treatment phase, and a post treatment follow-up phase.
An end-of-study visit will be conducted within 30 days after the last dose of SYHX2001.
Studietyp
Interventionell
Inskrivning (Förväntat)
176
Fas
- Fas 1
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Xiaodong Wang
- Telefonnummer: +86 021-60673947
- E-post: wang_xiaodong@mail.ecspc.com
Studieorter
-
-
Heilongjiang
-
Harbin, Heilongjiang, Kina
- Rekrytering
- Harbin Medical University Cancer Hospital
-
Kontakt:
- Yanqiao Zhang, Professor
- Telefonnummer: 13845120210
- E-post: yanqiaozhang@126.com
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
18 år till 75 år (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Nej
Kön som är behöriga för studier
Allt
Beskrivning
Inclusion Criteria:
- Male or female patients with an age of 18~75years (inclusive).
- Confirmed histologic or cytologic diagnosis of an advanced and/or metastatic solid tumor.
- At least one measurable lesion as defined by RECIST version 1.1.
- Eastern Cooperative Oncology Group Performance Status 0 or 1.
- Life expectancy ≥3 months.
- Major organ function within 14 days prior to treatment meets the following criteria (no blood transfusion, Erythropoietin(EPO), Granulocyte Colony Stimulating Factor(G-CSF) or other medical support): Absolute Neutrophil Count(ANC)≥1.5×10^9/L,Platelet(PLT)≥90×10^9/L,Hemoglobin(Hb)≥100g/L or≥6.2 mmol/L;Creatinine(Cr)≤1.5×upper limit of normal(ULN) and creatinine clearance rate≥50mL/min;Total Bilirubin(TBIL)≤1.5×ULN; Prothrombin time(PT)≤1.5×ULN , Activated Partial Thromboplastin Time(APTT)≤1.5×ULN , Aspartate Aminotransferase(AST)/Alanine Aminotransferase(ALT)≤2.5 × ULN.
- Signed informed consent form.
Exclusion Criteria:
- Chemotherapy, radiotherapy, biotherapy, endocrine therapy, targeted therapy, immunotherapy and other anti-tumor treatment within 4 weeks prior to the first dose of the study drug, or administration of other investigational agents within 4 weeks or 5 half-lives prior to the first dose of the study drug, whichever is longer.
- Major surgery or significant trauma within 4 weeks prior to the first dose of the study drug.
- Adverse reactions from the previous anti-tumor treatment have not yet recovered to ≤ level 1 based on CTCAE 5.0。
- Have a history of severe cardiovascular and cerebrovascular disease.
- Central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence shows that the patient's central nervous system metastasis or meningeal metastasis has not been controlled and not suitable for the study according to the judgment of the investigator.
- Known history of hypersensitivity to test drug components.
- Patients with recent active bleeding or a history of bleeding.
- Those with coagulation disorders or taking thrombolytic, anticoagulant or antiplatelet agglutination drugs.
- Gastrointestinal perforation, abdominal fistula, or intra-abdominal abscess within 6 months prior to first dose; or currently under investigator's judgement there are high risk factors for hollow organ perforation/fistula formation).
- Inability to swallow the drug orally, or a condition that seriously affects gastrointestinal absorption in the judgment of the investigator.
- Irritable bowel syndrome with signs/symptoms requiring medication.
- Persistent active diarrhea requiring medical treatment.
- Concomitant use of strong CYP3A4 inhibitors or inducers, strong CYP2D6 inhibitors and strong P-gp inhibitors within 14 days prior to the first dose of the study drug.
- History of autoimmune diseases, immunodeficiency, including HIV positive, or other acquired, congenital immunodeficiency, or organ transplant history.
- Known Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), or other active viral infection.
- Male and female patients of childbearing potential do not agree to use suitable method of contraception during the treatment and 6 months after the last dose of study medication; female patients do not have negative results of serum/urine pregnancy test within 7 days prior to enrollment and would be breastfeeding.
- Not suitable for this study as determined by the investigator due to other reasons.
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: SYHX2001
SYHX2001 will be administered orally.
|
SYHX2001 tablets, oral
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
Dose limiting toxicities (DLT) in stage Ⅰ
Tidsram: Baseline through Day 28
|
Baseline through Day 28
|
|
Maximum tolerated dose (MTD) in stage Ⅰ
Tidsram: Baseline through Day 28
|
Baseline through Day 28
|
|
Recommended phase 2 dose (RP2D)
Tidsram: Baseline through approximately 2 years
|
Baseline through approximately 2 years
|
|
Incidence and severity of adverse events in stage Ⅰ
Tidsram: Baseline through approximately 2 years
|
Baseline through approximately 2 years
|
|
Overall response rate (ORR) in stage Ⅱ
Tidsram: Up to approximately 2 years
|
Up to approximately 2 years
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Maximum observed plasma concentration (Cmax) of SYHX2001
Tidsram: Baseline and up to approximately 2 years
|
Baseline and up to approximately 2 years
|
|
|
Area under the plasma concentration-time curve (AUC) extrapolated from time zero to infinity (AUC[0-inf]) of SYHX2001
Tidsram: up to approximately 2 years
|
up to approximately 2 years
|
|
|
AUC from time zero to the last quantifiable concentration after dosing (AUC[0-t]) of SYHX2001
Tidsram: up to approximately 2 years
|
up to approximately 2 years
|
|
|
Terminal phase half-life (t1/2) of SYHX2001
Tidsram: up to approximately 2 years
|
up to approximately 2 years
|
|
|
Oral clearance (CL/F) of SYHX2001
Tidsram: up to approximately 2 years
|
up to approximately 2 years
|
|
|
PFS Progression-free survival (PFS)
Tidsram: up to approximately 2 years
|
PFS is defined as the time from first dose until radiographic progression per standard criteria or death due to any cause, whichever is earlier.
|
up to approximately 2 years
|
|
Duration of Response (DOR)
Tidsram: up to approximately 2 years
|
DOR is defined as the time from first evidence of response (complete response or partial response per RECIST 1.1) to earlier date of disease progression or death due to any cause.
|
up to approximately 2 years
|
|
Number of patients with any adverse events(AEs) and serious adverse events(SAEs) in stage Ⅱ
Tidsram: up to approximately 2 years
|
up to approximately 2 years
|
|
|
Change from Baseline in symmetrical arginine dimethylation (SDMA) as a pharmacodynamics(PD) measure
Tidsram: Baseline and up to approximately 2 years
|
Baseline and up to approximately 2 years
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
27 juli 2022
Primärt slutförande (Förväntat)
6 januari 2026
Avslutad studie (Förväntat)
6 januari 2026
Studieregistreringsdatum
Först inskickad
30 maj 2022
Först inskickad som uppfyllde QC-kriterierna
3 juni 2022
Första postat (Faktisk)
7 juni 2022
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
9 augusti 2022
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
8 augusti 2022
Senast verifierad
1 augusti 2022
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- SYHX2001C101
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